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Gene: PSMC4 |
Gene summary for PSMC4 |
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Gene information | Species | Human | Gene symbol | PSMC4 | Gene ID | 5704 |
Gene name | proteasome 26S subunit, ATPase 4 | |
Gene Alias | MIP224 | |
Cytomap | 19q13.2 | |
Gene Type | protein-coding | GO ID | GO:0001701 | UniProtAcc | A8K2M0 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
5704 | PSMC4 | CA_HPV_2 | Human | Cervix | CC | 2.45e-05 | 3.03e-01 | 0.0391 |
5704 | PSMC4 | Tumor | Human | Cervix | CC | 4.61e-10 | 3.65e-01 | 0.1241 |
5704 | PSMC4 | sample1 | Human | Cervix | CC | 5.47e-14 | 7.06e-01 | 0.0959 |
5704 | PSMC4 | sample3 | Human | Cervix | CC | 7.68e-08 | 3.11e-01 | 0.1387 |
5704 | PSMC4 | T1 | Human | Cervix | CC | 1.19e-14 | 5.29e-01 | 0.0918 |
5704 | PSMC4 | T3 | Human | Cervix | CC | 3.84e-07 | 2.90e-01 | 0.1389 |
5704 | PSMC4 | HTA11_2487_2000001011 | Human | Colorectum | SER | 5.34e-07 | 2.63e-01 | -0.1808 |
5704 | PSMC4 | HTA11_1938_2000001011 | Human | Colorectum | AD | 6.90e-04 | 2.58e-01 | -0.0811 |
5704 | PSMC4 | HTA11_347_2000001011 | Human | Colorectum | AD | 1.50e-09 | 2.59e-01 | -0.1954 |
5704 | PSMC4 | HTA11_411_2000001011 | Human | Colorectum | SER | 4.06e-04 | 5.70e-01 | -0.2602 |
5704 | PSMC4 | HTA11_3361_2000001011 | Human | Colorectum | AD | 9.73e-04 | 2.28e-01 | -0.1207 |
5704 | PSMC4 | HTA11_696_2000001011 | Human | Colorectum | AD | 3.09e-06 | 2.66e-01 | -0.1464 |
5704 | PSMC4 | HTA11_1391_2000001011 | Human | Colorectum | AD | 4.12e-13 | 3.65e-01 | -0.059 |
5704 | PSMC4 | HTA11_866_3004761011 | Human | Colorectum | AD | 4.49e-10 | 2.84e-01 | 0.096 |
5704 | PSMC4 | HTA11_7696_3000711011 | Human | Colorectum | AD | 7.30e-03 | 2.01e-01 | 0.0674 |
5704 | PSMC4 | HTA11_99999970781_79442 | Human | Colorectum | MSS | 3.03e-05 | 1.96e-01 | 0.294 |
5704 | PSMC4 | HTA11_99999965062_69753 | Human | Colorectum | MSI-H | 3.53e-02 | 7.05e-01 | 0.3487 |
5704 | PSMC4 | HTA11_99999965104_69814 | Human | Colorectum | MSS | 1.50e-05 | 2.48e-01 | 0.281 |
5704 | PSMC4 | HTA11_99999971662_82457 | Human | Colorectum | MSS | 1.31e-03 | 3.24e-01 | 0.3859 |
5704 | PSMC4 | HTA11_99999973899_84307 | Human | Colorectum | MSS | 3.40e-04 | 3.38e-01 | 0.2585 |
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∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage. |
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Malignant transformation related pathway analysis |
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Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | AD | ![]() |
Colorectum | SER | ![]() |
Colorectum | MSS | ![]() |
Colorectum | MSI-H | ![]() |
Colorectum | FAP | ![]() |
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:000182413 | Skin | cSCC | blastocyst development | 53/4864 | 106/18723 | 9.74e-08 | 2.32e-06 | 53 |
GO:0010498113 | Thyroid | PTC | proteasomal protein catabolic process | 297/5968 | 490/18723 | 4.58e-40 | 9.63e-37 | 297 |
GO:0043161113 | Thyroid | PTC | proteasome-mediated ubiquitin-dependent protein catabolic process | 254/5968 | 412/18723 | 3.91e-36 | 4.54e-33 | 254 |
GO:0009896113 | Thyroid | PTC | positive regulation of catabolic process | 278/5968 | 492/18723 | 3.35e-30 | 2.64e-27 | 278 |
GO:0031331113 | Thyroid | PTC | positive regulation of cellular catabolic process | 249/5968 | 427/18723 | 5.28e-30 | 3.58e-27 | 249 |
GO:0042176113 | Thyroid | PTC | regulation of protein catabolic process | 231/5968 | 391/18723 | 4.76e-29 | 2.14e-26 | 231 |
GO:1903362113 | Thyroid | PTC | regulation of cellular protein catabolic process | 162/5968 | 255/18723 | 1.62e-25 | 5.12e-23 | 162 |
GO:1903050113 | Thyroid | PTC | regulation of proteolysis involved in cellular protein catabolic process | 140/5968 | 221/18723 | 4.63e-22 | 1.01e-19 | 140 |
GO:0045732113 | Thyroid | PTC | positive regulation of protein catabolic process | 142/5968 | 231/18723 | 1.43e-20 | 2.38e-18 | 142 |
GO:0061136113 | Thyroid | PTC | regulation of proteasomal protein catabolic process | 121/5968 | 187/18723 | 2.25e-20 | 3.37e-18 | 121 |
GO:1903364113 | Thyroid | PTC | positive regulation of cellular protein catabolic process | 104/5968 | 155/18723 | 1.93e-19 | 2.39e-17 | 104 |
GO:0045862113 | Thyroid | PTC | positive regulation of proteolysis | 198/5968 | 372/18723 | 6.68e-18 | 6.91e-16 | 198 |
GO:1901800112 | Thyroid | PTC | positive regulation of proteasomal protein catabolic process | 80/5968 | 114/18723 | 4.80e-17 | 4.27e-15 | 80 |
GO:1903052112 | Thyroid | PTC | positive regulation of proteolysis involved in cellular protein catabolic process | 88/5968 | 133/18723 | 4.30e-16 | 3.39e-14 | 88 |
GO:0001701111 | Thyroid | PTC | in utero embryonic development | 175/5968 | 367/18723 | 1.40e-10 | 4.73e-09 | 175 |
GO:00018246 | Thyroid | PTC | blastocyst development | 49/5968 | 106/18723 | 1.37e-03 | 7.72e-03 | 49 |
GO:001049832 | Thyroid | ATC | proteasomal protein catabolic process | 309/6293 | 490/18723 | 1.78e-41 | 1.13e-37 | 309 |
GO:0043161210 | Thyroid | ATC | proteasome-mediated ubiquitin-dependent protein catabolic process | 265/6293 | 412/18723 | 7.09e-38 | 1.49e-34 | 265 |
GO:0009896210 | Thyroid | ATC | positive regulation of catabolic process | 290/6293 | 492/18723 | 2.15e-31 | 1.94e-28 | 290 |
GO:0031331210 | Thyroid | ATC | positive regulation of cellular catabolic process | 258/6293 | 427/18723 | 2.09e-30 | 1.65e-27 | 258 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0501220 | Cervix | CC | Parkinson disease | 102/1267 | 266/8465 | 1.81e-21 | 1.47e-19 | 8.66e-20 | 102 |
hsa0502018 | Cervix | CC | Prion disease | 98/1267 | 273/8465 | 2.64e-18 | 1.42e-16 | 8.42e-17 | 98 |
hsa0501018 | Cervix | CC | Alzheimer disease | 113/1267 | 384/8465 | 9.67e-14 | 3.92e-12 | 2.32e-12 | 113 |
hsa0501618 | Cervix | CC | Huntington disease | 94/1267 | 306/8465 | 8.49e-13 | 3.06e-11 | 1.81e-11 | 94 |
hsa0502218 | Cervix | CC | Pathways of neurodegeneration - multiple diseases | 128/1267 | 476/8465 | 2.87e-12 | 9.29e-11 | 5.50e-11 | 128 |
hsa0501418 | Cervix | CC | Amyotrophic lateral sclerosis | 103/1267 | 364/8465 | 1.79e-11 | 4.47e-10 | 2.64e-10 | 103 |
hsa0516920 | Cervix | CC | Epstein-Barr virus infection | 57/1267 | 202/8465 | 7.30e-07 | 7.39e-06 | 4.37e-06 | 57 |
hsa0305014 | Cervix | CC | Proteasome | 16/1267 | 46/8465 | 6.69e-04 | 3.09e-03 | 1.83e-03 | 16 |
hsa0501716 | Cervix | CC | Spinocerebellar ataxia | 35/1267 | 143/8465 | 1.77e-03 | 7.21e-03 | 4.26e-03 | 35 |
hsa05012110 | Cervix | CC | Parkinson disease | 102/1267 | 266/8465 | 1.81e-21 | 1.47e-19 | 8.66e-20 | 102 |
hsa0502019 | Cervix | CC | Prion disease | 98/1267 | 273/8465 | 2.64e-18 | 1.42e-16 | 8.42e-17 | 98 |
hsa0501019 | Cervix | CC | Alzheimer disease | 113/1267 | 384/8465 | 9.67e-14 | 3.92e-12 | 2.32e-12 | 113 |
hsa0501619 | Cervix | CC | Huntington disease | 94/1267 | 306/8465 | 8.49e-13 | 3.06e-11 | 1.81e-11 | 94 |
hsa0502219 | Cervix | CC | Pathways of neurodegeneration - multiple diseases | 128/1267 | 476/8465 | 2.87e-12 | 9.29e-11 | 5.50e-11 | 128 |
hsa0501419 | Cervix | CC | Amyotrophic lateral sclerosis | 103/1267 | 364/8465 | 1.79e-11 | 4.47e-10 | 2.64e-10 | 103 |
hsa05169110 | Cervix | CC | Epstein-Barr virus infection | 57/1267 | 202/8465 | 7.30e-07 | 7.39e-06 | 4.37e-06 | 57 |
hsa0305015 | Cervix | CC | Proteasome | 16/1267 | 46/8465 | 6.69e-04 | 3.09e-03 | 1.83e-03 | 16 |
hsa0501717 | Cervix | CC | Spinocerebellar ataxia | 35/1267 | 143/8465 | 1.77e-03 | 7.21e-03 | 4.26e-03 | 35 |
hsa05012 | Colorectum | AD | Parkinson disease | 147/2092 | 266/8465 | 2.53e-27 | 8.48e-25 | 5.41e-25 | 147 |
hsa05010 | Colorectum | AD | Alzheimer disease | 174/2092 | 384/8465 | 1.82e-19 | 9.26e-18 | 5.91e-18 | 174 |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression. |
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Somatic mutation of malignant transformation related genes |
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Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
PSMC4 | SNV | Missense_Mutation | c.481N>C | p.Asp161His | p.D161H | P43686 | protein_coding | deleterious(0.01) | possibly_damaging(0.77) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
PSMC4 | SNV | Missense_Mutation | c.565N>A | p.Glu189Lys | p.E189K | P43686 | protein_coding | deleterious(0.02) | benign(0.098) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
PSMC4 | SNV | Missense_Mutation | c.383N>T | p.Ala128Val | p.A128V | P43686 | protein_coding | tolerated(0.18) | benign(0.283) | TCGA-B6-A0I8-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | PD | |
PSMC4 | SNV | Missense_Mutation | c.1154T>C | p.Leu385Ser | p.L385S | P43686 | protein_coding | tolerated(0.27) | benign(0.071) | TCGA-D8-A142-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | cyclophosphamid | SD | |
PSMC4 | SNV | Missense_Mutation | c.646N>A | p.Ala216Thr | p.A216T | P43686 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-E2-A150-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD | |
PSMC4 | SNV | Missense_Mutation | novel | c.970C>T | p.Pro324Ser | p.P324S | P43686 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-LL-A5YP-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD |
PSMC4 | SNV | Missense_Mutation | c.565N>A | p.Glu189Lys | p.E189K | P43686 | protein_coding | deleterious(0.02) | benign(0.098) | TCGA-AA-3846-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
PSMC4 | SNV | Missense_Mutation | c.617N>T | p.Gly206Val | p.G206V | P43686 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-F4-6856-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Ancillary | leucovorin | CR | |
PSMC4 | insertion | Frame_Shift_Ins | rs765768285 | c.598dupC | p.Arg200ProfsTer43 | p.R200Pfs*43 | P43686 | protein_coding | TCGA-G4-6588-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
PSMC4 | SNV | Missense_Mutation | c.1016G>A | p.Arg339His | p.R339H | P43686 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
5704 | PSMC4 | NA | CARFILZOMIB | CARFILZOMIB | 24524217 | |
5704 | PSMC4 | NA | inhibitor | CARFILZOMIB | CARFILZOMIB | |
5704 | PSMC4 | NA | inhibitor | CHEMBL2103884 | OPROZOMIB | |
5704 | PSMC4 | NA | inhibitor | BORTEZOMIB | BORTEZOMIB | |
5704 | PSMC4 | NA | inhibitor | CHEMBL3545432 | IXAZOMIB CITRATE | |
5704 | PSMC4 | NA | BORTEZOMIB | BORTEZOMIB | 24524217 | |
5704 | PSMC4 | NA | inhibitor | CHEMBL451887 | CARFILZOMIB | |
5704 | PSMC4 | NA | inhibitor | CHEMBL325041 | BORTEZOMIB |
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